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作 者:靳波[1,2] 刘友平[1,2] 陈鸿平[1,2] 赵祎姗[1,2] 彭月[1,2]
机构地区:[1]成都中医药大学药学院,四川成都611137 [2]中药资源系统研究与开发利用省部共建国家重点实验室培育基地,四川成都611137
出 处:《四川中医》2011年第3期66-68,共3页Journal of Sichuan of Traditional Chinese Medicine
基 金:质检公益性行业科研专项(No.2007GYB075-2);校学生科研实践创新课题(013-011-39)
摘 要:目的:从升麻中分离得到升麻苷H-1并建立其定量测定方法。方法:采用硅胶柱色谱从升麻乙醇提取液的水不溶性部位分离得到升麻苷H-1;采用HPLC法,色谱柱:Hypersil BDS C18柱(200mm×4.6mm,5μm),流动相:甲醇-水(60∶40),检测波长:210nm,流速:1.0ml/min,柱温:30℃。结果:升麻苷-1在0.358~6.444mg范围内呈现良好的线性关系(r=0.9996),精密度、稳定性和重现性的RSD均小于2%,平均加样回收率为101.9%,RSD为4.81%。结论:该方法准确、快速、重现性好,可用于测定升麻药材中升麻苷H-1的含量。Objective:To establish an accurate method for the determination of Cimicifugoside H-1which was isolated from Cimicifugae Rhizome.Methods:Cimicifugoside H-1 was isolated from water-insoluble part of Cimicifuga ethanol extract by silica gel column chromatography;HPLC analysis was performed on Hypersil BDS C18 column(200mm×4.6mm,5μm)with a mobile phase consisting of methanol:water(60∶40).The flow rate was 1.0ml/min.The detection wavelength was 210 nm and the column temperature was 30℃.Results:The linear range of Cimicifugoside H-1 was within 0.358~6.444 mg(r=0.9996).The results that RSD of precision,stability,reproducibility were all less than 2%.The average recovery was 101.9% and RSD was 4.81%.Conclusions:The method is simple and accurate and can be used for determinating Cimicifugoside H-1 of Cimicifugae.
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